JPH0219100B2 - - Google Patents
Info
- Publication number
- JPH0219100B2 JPH0219100B2 JP55088007A JP8800780A JPH0219100B2 JP H0219100 B2 JPH0219100 B2 JP H0219100B2 JP 55088007 A JP55088007 A JP 55088007A JP 8800780 A JP8800780 A JP 8800780A JP H0219100 B2 JPH0219100 B2 JP H0219100B2
- Authority
- JP
- Japan
- Prior art keywords
- prenol
- reaction
- citral
- boiling point
- column
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 claims description 26
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 claims description 17
- 238000009835 boiling Methods 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 17
- 229940043350 citral Drugs 0.000 claims description 17
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 claims description 17
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 8
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 6
- 239000003377 acid catalyst Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000012442 inert solvent Substances 0.000 claims description 4
- NSPPRYXGGYQMPY-UHFFFAOYSA-N 3-Methylbuten-2-ol-1 Natural products CC(C)C(O)=C NSPPRYXGGYQMPY-UHFFFAOYSA-N 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- FMTWOCDQSALHMT-UHFFFAOYSA-N 3-methyl-1-(3-methylbuta-1,3-dienoxy)but-2-ene Chemical compound CC(C)=CCOC=CC(C)=C FMTWOCDQSALHMT-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 150000001993 dienes Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000543 intermediate Substances 0.000 description 18
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- OSDSMAURJWMWHY-UHFFFAOYSA-N 3-methyl-1-(2-methylbut-3-en-2-yloxy)but-2-ene Chemical compound CC(C)=CCOC(C)(C)C=C OSDSMAURJWMWHY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AUFZRCJENRSRLY-UHFFFAOYSA-N 2,3,5-trimethylhydroquinone Chemical compound CC1=CC(O)=C(C)C(C)=C1O AUFZRCJENRSRLY-UHFFFAOYSA-N 0.000 description 1
- QWQNFXDYOCUEER-UHFFFAOYSA-N 2,3-ditert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1C(C)(C)C QWQNFXDYOCUEER-UHFFFAOYSA-N 0.000 description 1
- QGZMQPRJYZVDKE-UHFFFAOYSA-N 2-methyl-4-(2-methylbut-3-en-2-yloxy)but-1-ene Chemical compound CC(=C)CCOC(C)(C)C=C QGZMQPRJYZVDKE-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- -1 methyl-3-buten-1-al-diprenyl acetal Chemical compound 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/515—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792926562 DE2926562A1 (de) | 1979-06-30 | 1979-06-30 | Verfahren zur herstellung von citral |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5610128A JPS5610128A (en) | 1981-02-02 |
| JPH0219100B2 true JPH0219100B2 (de) | 1990-04-27 |
Family
ID=6074654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8800780A Granted JPS5610128A (en) | 1979-06-30 | 1980-06-30 | Manufacture of citral |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4288636A (de) |
| EP (1) | EP0021074B1 (de) |
| JP (1) | JPS5610128A (de) |
| DE (2) | DE2926562A1 (de) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4400550A (en) * | 1982-02-12 | 1983-08-23 | Albany International Corp. | Synthesis of the navel orange worm pheromone (Z,Z)-11,13-hexadecadienal |
| FR2631337B1 (fr) * | 1988-05-16 | 1990-07-27 | Rhone Poulenc Sante | Procede de preparation du citral |
| US5017726A (en) * | 1988-11-09 | 1991-05-21 | Union Camp Corporation | Processes for the conversion of myrcene to nerol and citral |
| FR2656604B1 (fr) * | 1990-01-03 | 1992-03-20 | Rhone Poulenc Sante | Procede de preparation du citral. |
| FR2661408B1 (fr) * | 1990-04-27 | 1993-09-17 | Rhone Poulenc Nutrition Animal | Procede de preparation de citral. |
| US5094720A (en) * | 1990-10-18 | 1992-03-10 | Union Camp Corporation | Process for the distillative purification of citral |
| DE19846056A1 (de) * | 1998-10-07 | 2000-04-13 | Basf Ag | Verfahren zur Herstellung von Citral |
| US6278016B1 (en) | 1999-12-09 | 2001-08-21 | Loyola University Of Chicago | Methods for conversion of isoprene to prenyl alcohol and related compounds |
| EP2008989A1 (de) * | 2007-06-26 | 2008-12-31 | Basf Se | Kontinuierliches Verfahren zur Herstellung von Neral in reiner oder angereicherter Form |
| CN103787852B (zh) * | 2014-01-23 | 2015-06-10 | 万华化学集团股份有限公司 | 一种柠檬醛的制备方法 |
| CN106977383B (zh) * | 2017-03-10 | 2020-04-10 | 万华化学集团股份有限公司 | 一种制备柠檬醛的方法 |
| CN111018682A (zh) * | 2019-12-17 | 2020-04-17 | 南通天泽化工有限公司 | 一种柠檬醛的制备方法 |
| CN111807936B (zh) * | 2020-07-22 | 2022-11-08 | 万华化学集团股份有限公司 | 一种异戊二烯基异戊烯基醚的制备方法 |
| CN113979843A (zh) * | 2021-09-23 | 2022-01-28 | 国药集团威奇达药业有限公司 | 一种直接催化裂解制备烯基醚的方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2501144A (en) * | 1947-12-19 | 1950-03-21 | Hercules Powder Co Ltd | Unsaturated aldehydes and preparation thereof |
| JPS49125314A (de) * | 1973-03-12 | 1974-11-30 | ||
| JPS5012009A (de) * | 1973-05-14 | 1975-02-07 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2987551A (en) * | 1958-06-06 | 1961-06-06 | Eastman Kodak Co | Preparation of citral |
| FR1524289A (fr) * | 1967-03-29 | 1968-05-10 | Melle Usines Sa | Procédé de scission d'acétals |
| DE2157035C3 (de) * | 1971-11-17 | 1974-07-04 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung höhermolekularer alpha-beta-ungesättigter Aldehyde |
| US4016212A (en) * | 1973-03-12 | 1977-04-05 | Hoffmann-La Roche Inc. | Process for the preparation of aldehydes |
| US4123464A (en) * | 1973-03-12 | 1978-10-31 | Hoffmann-La Roche Inc. | Process for the preparation of aldehydes |
| US3978092A (en) * | 1973-05-14 | 1976-08-31 | Teijin Limited | Process for the preparation of unsaturated carbonyl compounds |
| AU7218574A (en) * | 1973-08-16 | 1976-02-12 | Teijin Ltd | Unsaturated carbonyl compounds |
| FR2335483A1 (fr) * | 1975-12-19 | 1977-07-15 | Rhone Poulenc Ind | Preparation de citral |
-
1979
- 1979-06-30 DE DE19792926562 patent/DE2926562A1/de not_active Withdrawn
-
1980
- 1980-05-27 DE DE8080102940T patent/DE3060336D1/de not_active Expired
- 1980-05-27 EP EP80102940A patent/EP0021074B1/de not_active Expired
- 1980-06-10 US US06/158,346 patent/US4288636A/en not_active Expired - Lifetime
- 1980-06-30 JP JP8800780A patent/JPS5610128A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2501144A (en) * | 1947-12-19 | 1950-03-21 | Hercules Powder Co Ltd | Unsaturated aldehydes and preparation thereof |
| JPS49125314A (de) * | 1973-03-12 | 1974-11-30 | ||
| JPS5012009A (de) * | 1973-05-14 | 1975-02-07 |
Also Published As
| Publication number | Publication date |
|---|---|
| US4288636A (en) | 1981-09-08 |
| JPS5610128A (en) | 1981-02-02 |
| DE2926562A1 (de) | 1981-01-22 |
| EP0021074A1 (de) | 1981-01-07 |
| EP0021074B1 (de) | 1982-04-28 |
| DE3060336D1 (en) | 1982-06-09 |
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